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31 de mar. de 2024 · Databases. The MAUDE database houses medical device reports submitted to the FDA by mandatory reporters 1 (manufacturers, importers and device user facilities) and voluntary reporters such as...
- Standards
Medical Device Reports (MAUDE) CDRH Export Certificate...
- CLIA
Aquí nos gustaría mostrarte una descripción, pero el sitio...
- Adverse Events
The Manufacturer and User Facility Device Experience (MAUDE)...
- Download Files
This page contains information about Manufacturer and User...
- MDR Data Files Webpage
Like all MDR data in MAUDE, MDR data in ASR reports cannot...
- Cdrh FOIA Electronic Reading Room
Aquí nos gustaría mostrarte una descripción, pero el sitio...
- FDA Guidance Documents
Some FDA guidance documents on this list are indicated as...
- Post-Approval Studies
Mandated Studies Program Food and Drug Administration 10903...
- Standards
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31 de mar. de 2024 · The MAUDE database houses medical device reports submitted to the FDA by mandatory reporters 1 (manufacturers, importers and device user facilities) and voluntary reporters such as health care professionals, patients and consumers.
